Clinical Research Coordinator I — Data, Consent & Study Support

Mount Sinai Morningside; New York (NY); On-site; USD 59,000 - 74,000; Full time

Job summary

Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist with grant applications and IRB-related documents.

Responsibilities include maintaining source documents, handling specimens, and preparing for monitoring visits, ensuring compliance with hospital procedures and regulatory requirements.

Qualifications

• Bachelor's or Master's degree in Science or closely related field.
• No experience required; one year of research experience preferred.

Responsibilities

• Collects and records study data and inputs into the database.
• Obtains informed consent and educates participants about study requirements.
• Assists with grant applications, IRB submissions, and related filings.
• Maintains source documents and subject files per procedures.
• Ships and delivers clinical specimens as required by protocol.
• Prepares for monitoring visits and conducts related duties.

Skills

Informed consent

Data collection

Study coordination

Communication

Education

Bachelor's or Master's degree in Science or related field

Tools

Database management

Grant applications

Job description

Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily activities of clinical studies. You will obtain informed consent, collect and organize study data, and assist with grant applications and IRB-related documents.

Responsibilities include maintaining source documents, handling specimens, and preparing for monitoring visits, ensuring compliance with hospital procedures and regulatory requirements.